| Tag | Content |
|---|
EnhancerAtlas ID | HS197-11236 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr2:26852680-26855430 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr2:26853267-26853282 | AGGGCTGTGTGACCT | - | 6.51 | | NFYB | MA0502.1 | chr2:26854023-26854038 | CTGATTGGTGGAATT | - | 6.05 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I026631 | chr2 | 26853921 | 26854070 |
|
Enhancer Sequence | CGAGGGTTCA TCATAGAATG TCAGAACTGA AGGGGCTTAT GTCCAGTCCC TCGGTTACGG 60
ATGGGGAAGC CAGTAGGACC TTGGGGAAGC CAGGGTCCCC ACCTCTGGCC ATCTGCCAAT 120
TTCCATCCTC AACCCAAGAA AAGAGGTCAC TTCGTGGGTC TGAGTGAGCC GGGATTAGAG 180
CCCGGCTGCC TGCAGCCAGC AAACCACCAG CCTTGCTAGG CCACTTGACA GCAAACTTGG 240
TTGCAGCAGA TCGTGGACTG ACTGGTCTTC CTAATCATCC CTGTCAGCGA TGTCTCTTGT 300
CTATAGGATC CCATCCCAGT CAAGAGGATT TTGCTTATAA GCTACAGGCA GAGGGTGAAA 360
TGGCCGTGTG ACCCCTGAGA GTAAGAGGGC GGGAGGGAGC TCTGCCTCAG GCTAAGAGAG 420
GATGAGCCCT CATTGCCTGT CTCTCTCACC CTATCCTGAA CCTGGGTCCC TGTCCACCAG 480
CAAGCTCTTA GGCCTACAGG TCCAGCACCC AAGGCAGCCA GTGGAGGTGA GACAGTGGTG 540
CCCTGGGGCC CAGGAGGCCT GGATCCCAGA ACCTGAACTG CTGTGGCAGG GCTGTGTGAC 600
CTCGGGCAAC TCACTTGACA TTTCTGAACT TTAGTTTCAT CATCTGGATA AGGGACAAGA 660
ATGATATGTC TCTTGGAGGG CTGTGGCGGG GGTTCAGTGT GAAGGAGGCT GAAGGGTATG 720
TGTGTTTATG TATAAATGGT GGATGGCGGG TGGTGGGGTC ACCACAGGCT GGTTGAAAAC 780
ACTGTCTCTA GAGCCGGACA GATCTACATT CAAATCCTGA CTCTGCCACT TAATAGTTCT 840
GAGGCGTCGA GCAAGGTTCT GAATCCACCT GAGCCTCAGT CTGCTCCTCT TTGCAGTGGG 900
GTAGTAAATC TCCCCCCACA CACTCGTGAG GATTAAATGA GGGGAGGTGT ATGAAACGTC 960
AGCGCAGTGT TTGGTAGGTA AGAGTGTTTG TGTTACCCGG GGCCTCAGAG GGGACACCCA 1020
GCCTGCCCTC TCTCTGTGTT TCTCTCCTAT ACTCCAGGTG CCCCTGTGCT CCTGGGCTGT 1080
GCACAACCCA CACCTAGACT GTGAGAGTGG GAGCCCACCA CCCTGACCCA GACCTGCTCT 1140
CCCCTCTCTT CATGGTCCCC TCCATGCTCC AAAATTACCC CTCCCTCCTT TAGTCCTTTC 1200
CTGTTCCTCT CCTGTCTTCC ATCAAACCTC TACTCTCCTG AGAGGCCAGC AATCCCATGA 1260
AAGGAGTCTG TATGCAGGAG TGAGTGACTA ACAGTCCCCT ATTGACATTC CAGGGTATGT 1320
GGTTTGTTGA CTCAAATGAG GCTCTGATTG GTGGAATTTA GGGACATGTA ACTAAGTGAA 1380
GACCGGGTGC GGCGGCTCAT ACCAGTAATC CCAGCCCTTC AGGAGGCTGA GGCGGGAGAA 1440
TCGCTTGAGC CCAAGAGTTT GAGACCACCC TAGGCAATAC AGGGAGACCC CATTTCTACA 1500
AAAAAATTGA AAATTAGCCA GGCATACTGG CACGCACCTA TAGTCTAGCT ATTCAGGAGG 1560
CTGAAGTGGG AGGATCACTG GATCCCAGGA GGTTGAGGCT GCAGCGAGCT GTGATCGCAC 1620
TACTGCACTC CAGCCTGGGC GACAGAGCAA GACCCCGTCT CAATAAACAA CAAAAACTAG 1680
GTGAAGAATT TGGAGGGTGA TTTTAGGAGT GGAGACTCAG AGGTAGAGCA GGAAGCAGGA 1740
GGCTCTCCCA GAGCCCTGAC GATGGTAGGT GGAGGCCTCG CACCCTGCCA GCCACTCACT 1800
GTTTCACATC TCACTGACTA GAAAAACATC CTTCAGCTCC CAGCCCTGGG AGAGTGGAAA 1860
GAAACTATGC TGGGATTCTG TGTGCCCACT GCACTCTGTG CCCTGGGAGG CTGATCTCTA 1920
CTGACAGTGT TCCCACCTCC CTTTCCCTCT GGCTTAAGGG AAGCTCCAGG AGGACTGGAG 1980
GTATGAGGGA TGGGTGGGGA TTTATCCTCC TCTCCCTCCC AGCCCCACAC GACTCTGCAG 2040
TGTCTGTGTT CCCGCTGTCT CAGGCTAGCA GCCAGCTTCT GCAGCTCCAG CTCTCAGCTA 2100
TCACCTCAGG CCTGGGGCAG TCAGGGCTGG CCCCTGGGTG CTTCCCTGGG CCTCCTTCTG 2160
AACAGTTCCT TCACTGCAAA GCACCTTCAA AGATCCTGCT GAGTGTGCCA CCTGCTTCCC 2220
GCCGGGTTGC TCACAGACCT ATCTGGATCT ATCTGGATCC TATTTCTCTA CCTCTAGCTA 2280
CGAGACCCAA GGCAAACTGC CGGACCTCTC TGAGCACGCA GGCCCAGGTT CATATCCTGA 2340
CTCTGTCTGA TGGAGAGCCA GCCTCCTTCC AGTGGCATTG TGCAGATCCA GGCTAGGGCC 2400
TGACAGATGG GAGCTGGAGT GGCGTGTGGT GTTCATGGAG AGCACCATGA CTGCCGCCTT 2460
GGCCACGGAA GGGGCCTGAG CTGTCACTAG GGTCTAGAGA CTGCACACGT TTGGGAGGGA 2520
GCAGAAAGCA GAGTGTGGAA CGGGTTGGGG GAGAGATTCT CCAGGAAAGT ACTGGGGTGG 2580
ATGCTGGGAA CCACAGGTCA ACAAGCAGGA AGAAAAGCCA TCACTGCTGA AGTGTCCAGT 2640
GGCCTACAAG GGGCGAGGGG TAGGCCGGGT GCAGTGGCTC CTGCCTGTAA TCCCAGCACT 2700
ATGGGAGGCT GAGGCAGGCG GATCACTGGA GGTCAGGAGT TCGAGAGCAG 2750
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